Genome‐wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21‐q22 von Cropp, Cheryl D., Simpson, Claire L, Wahlfors, Tiina, Ha, Nati, George, Asha, Jones, MaryPat S., Harper, Ursula, Ponciano‐Jackson, Damaris, Green, Tiffany A., Tammela, Teuvo L. J., Bailey‐Wilson, Joan, Schleutker, Johanna

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Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis von Simpson, Claire L, Cropp, Cheryl D, Wahlfors, Tiina, George, Asha, Jones, Marypat S, Harper, Ursula, Ponciano-Jackson, Damaris, Tammela, Teuvo, Schleutker, Johanna, Bailey-Wilson, Joan E

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Genome-wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3 von Wiklund, Fredrik, Gillanders, Elizabeth M., Albertus, Julie A., Bergh, Anders, Damber, Jan-Erik, Emanuelsson, Monica, Freas-Lutz, Diana L., Gildea, Derek E., Göransson, Ingela, Jones, MaryPat S., Jonsson, Björn-Anders, Lindmark, Fredrik, Markey, Carol J., Riedesel, Erica L., Stenman, Elisabeth, Trent, Jeffry M., Grönberg, Henrik

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Abstract 3648: Unraveling phenotype heterogeneity in prostate cancer susceptibility in Finland utilizing covariate-based analysis von Cropp, Cheryl D., Simpson, Claire L., Wahlfors, Tiina, George, Asha, Jones, MaryPat S., Harper, Ursula, Ponciano-Jackson, Damaris, Tammela, Teuvo, Schleutker, Johanna, Bailey-Wilson, Joan E.

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High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9 von Varshney, Gaurav K, Pei, Wuhong, LaFave, Matthew C, Idol, Jennifer, Xu, Lisha, Gallardo, Viviana, Carrington, Blake, Bishop, Kevin, Jones, MaryPat, Li, Mingyu, Harper, Ursula, Huang, Sunny C, Prakash, Anupam, Chen, Wenbiao, Sood, Raman, Ledin, Johan, Burgess, Shawn M

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A high-throughput functional genomics workflow based on CRISPR/Cas9-mediated targeted mutagenesis in zebrafish von Varshney, Gaurav K, Carrington, Blake, Pei, Wuhong, Bishop, Kevin, Chen, Zelin, Fan, Chunxin, Xu, Lisha, Jones, Marypat, LaFave, Matthew C, Ledin, Johan, Sood, Raman, Burgess, Shawn M

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Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility von Ramanagoudr-Bhojappa, Ramanagouda, Carrington, Blake, Ramaswami, Mukundhan, Bishop, Kevin, Robbins, Gabrielle M, Jones, MaryPat, Harper, Ursula, Frederickson, Stephen C, Kimble, Danielle C, Sood, Raman, Chandrasekharappa, Settara C

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Brain-Derived Neurotrophic Factor and Obesity in the WAGR Syndrome von Han, Joan C, Liu, Qing-Rong, Jones, MaryPat, Levinn, Rebecca L, Menzie, Carolyn M, Jefferson-George, Kyra S, Adler-Wailes, Diane C, Sanford, Ethan L, Lacbawan, Felicitas L, Uhl, George R, Rennert, Owen M, Yanovski, Jack A

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Efficient methods for targeted mutagenesis in zebrafish using zinc-finger nucleases: data from targeting of nine genes using CompoZr or CoDA ZFNs von Sood, Raman, Carrington, Blake, Bishop, Kevin, Jones, MaryPat, Rissone, Alberto, Candotti, Fabio, Chandrasekharappa, Settara C, Liu, Paul

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Reticular dysgenesis-associated AK2 protects hematopoietic stem and progenitor cell development from oxidative stress von Rissone, Alberto, Weinacht, Katja Gabriele, la Marca, Giancarlo, Bishop, Kevin, Giocaliere, Elisa, Jagadeesh, Jayashree, Felgentreff, Kerstin, Dobbs, Kerry, Al-Herz, Waleed, Jones, Marypat, Chandrasekharappa, Settara, Kirby, Martha, Wincovitch, Stephen, Simon, Karen Lyn, Itan, Yuval, DeVine, Alex, Schlaeger, Thorsten, Schambach, Axel, Sood, Raman, Notarangelo, Luigi D, Candotti, Fabio

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Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p von Gunay-Aygun, Meral, Zivony-Elboum, Yifat, Gumruk, Fatma, Geiger, Dan, Cetin, Mualla, Khayat, Morad, Kleta, Robert, Kfir, Nehama, Anikster, Yair, Chezar, Judith, Arcos-Burgos, Mauricio, Shalata, Adel, Stanescu, Horia, Manaster, Joseph, Arat, Mutlu, Edwards, Hailey, Freiberg, Andrew S., Hart, P. Suzanne, Riney, Lauren C., Patzel, Katherine, Tanpaiboon, Pranoot, Markello, Tom, Huizing, Marjan, Maric, Irina, Horne, McDonald, Kehrel, Beate E., Jurk, Kerstin, Hansen, Nancy F., Cherukuri, Praveen F., Jones, Marypat, Cruz, Pedro, Mullikin, Jim C., Nurden, Alan, White, James G., Gahl, William A., Falik-Zaccai, Tzippora

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A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase von Sei, Yoshitatsu, Zhao, Xilin, Forbes, Joanne, Szymczak, Silke, Li, Qing, Trivedi, Apurva, Voellinger, Mark, Joy, Grishma, Feng, Jianying, Whatley, Millie, Jones, MaryPat Sussex, Harper, Ursula L, Marx, Stephen J, Venkatesan, Aradhana M, Chandrasekharappa, Settara C, Raffeld, Mark, Quezado, Martha M, Louie, Adeline, Chen, Clara C, Lim, Ramona M, Agarwala, Richa, Schäffer, Alejandro A, Hughes, Marybeth S, Bailey-Wilson, Joan E, Wank, Stephen A

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CBFβ and RUNX1 are required at 2 different steps during the development of hematopoietic stem cells in zebrafish von Bresciani, Erica, Carrington, Blake, Wincovitch, Stephen, Jones, MaryPat, Gore, Aniket V., Weinstein, Brant M., Sood, Raman, Liu, P. Paul

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The vitamin B12 processing enzyme, mmachc, is essential for zebrafish survival, growth and retinal morphology von Sloan, Jennifer L, Achilly, Nathan P, Arnold, Madeline L, Catlett, Jerrel L, Blake, Trevor, Bishop, Kevin, Jones, Marypat, Harper, Ursula, English, Milton A, Anderson, Stacie, Trivedi, Niraj S, Elkahloun, Abdel, Hoffmann, Victoria, Brooks, Brian P, Sood, Raman, Venditti, Charles P

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Additive reductions in zebrafish PRPS1 activity result in a spectrum of deficiencies modeling several human PRPS1-associated diseases von Pei, Wuhong, Xu, Lisha, Varshney, Gaurav K., Carrington, Blake, Bishop, Kevin, Jones, MaryPat, Huang, Sunny C., Idol, Jennifer, Pretorius, Pamela R., Beirl, Alisha, Schimmenti, Lisa A., Kindt, Katie S., Sood, Raman, Burgess, Shawn M.

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Methods for reverse genetic screening in zebrafish by resequencing and TILLING von Sood, Raman, English, Milton A., Jones, MaryPat, Mullikin, James, Wang, Duen-Mei, Anderson, Maria, Wu, Dongying, Chandrasekharappa, Settara C., Yu, Jun, Zhang, Jinghui, Paul Liu, P.

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Development of RUNX1-Independent Hematopoiesis in Three Zebrafish runx1 -KO Models von Bresciani, Erica, Carrington, Blake, Kwon, Erika Mijin, Jones, Marypat, Bishop, Kevin, Broadbridge, Elizabeth, Dell'Orso, Stefania, Sood, Raman B., Liu, Paul P

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Development of Multi-Lineage Hematopoiesis in Two Novel Zebrafish runx1 mutants von Bresciani, Erica, Carrington, Blake, Kwon, Erika Mijin, Jones, Marypat, Wincovitch, Stephen, Sood, Raman B., Liu, Paul P.

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Guided genetic screen to identify genes essential in the regeneration of hair cells and other tissues von Pei, Wuhong, Xu, Lisha, Huang, Sunny C., Pettie, Kade, Idol, Jennifer, Rissone, Alberto, Jimenez, Erin, Sinclair, Jason W., Slevin, Claire, Varshney, Gaurav K., Jones, MaryPat, Carrington, Blake, Bishop, Kevin, Huang, Haigen, Sood, Raman, Lin, Shuo, Burgess, Shawn M.

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Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia von Donovan, Frank X., Kimble, Danielle C., Kim, Yonghwan, Lach, Francis P., Harper, Ursula, Kamat, Aparna, Jones, MaryPat, Sanborn, Erica M., Tryon, Rebecca, Wagner, John E., MacMillan, Margaret L., Ostrander, Elaine A., Auerbach, Arleen D., Smogorzewska, Agata, Chandrasekharappa, Settara C.

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